临床肿瘤学杂志

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阿瑞匹坦预防含铂类化疗方案治疗肺癌所致恶心呕吐的临床观察

李慎柯1,安彤同2   

  1. 1 457001 河南濮阳 濮阳市油田总医院肿瘤科2 100142 北京大学临床肿瘤学院
  • 收稿日期:2016-08-15 修回日期:2016-10-07 出版日期:2017-01-30 发布日期:2017-01-30
  • 通讯作者: 安彤同

Clinical observation of aprepitant for prevention of nausea and vomiting induced by platinum-based chemotherapy in lung cancer patients

LI Shenke, AN Tongtong.
  

  1. Department of Oncology, General Hospital of Puyang Oil Field, Puyang 457001, China
  • Received:2016-08-15 Revised:2016-10-07 Online:2017-01-30 Published:2017-01-30
  • Contact: AN Tongtong

摘要: 目的 探讨阿瑞匹坦在预防肺癌含铂化疗方案所致的化疗相关性恶心、呕吐的疗效和安全性。方法 收集2014年1月至2014年12月应用一线含铂化疗方案治疗的肺癌患者44例,采用自身对照比较使用阿瑞匹坦与否在化疗过程中止吐效果的差异,同时观察阿瑞匹坦在多周期化疗中的止吐疗效。结果 44例患者中,格拉司琼联合地塞米松组(A组)急性呕吐的发生率为50.0%,延迟性呕吐的发生率为81.8%;阿瑞匹坦、格拉司琼联合地塞米松组(B组)急性呕吐的发生率为25.0%,延迟性呕吐的发生率为47.7%;与A组相比,B组对急性呕吐的治疗有效率(RR)为909%,对延迟性呕吐的RR为77.8%。多周期化疗中阿瑞匹坦维持止吐效果较好,且无疗效衰减现象。阿瑞匹坦引起的不良反应主要有厌食、疲乏、便秘、腹泻,A组厌食的发生率为93.2%,高于B组的63.6%(P=0.001);两组其他不良反应发生率的差异无统计学意义(P>0.05)。结论 阿瑞匹坦可有效降低含铂化疗方案的急性和延迟性恶心呕吐的发生率,不良反应可耐受。

Abstract: Objective To evaluate the efficacy and tolerance of aprepitant on the prevention of nausea and vomiting induced by platinum-based chemotherapy in the treatment of patients with lung cancer. Methods A total of 44 cases of patients with lung cancer treated by platinum-based chemotherapy enrolled from January 2014 to December 2014 in Department of Thoracic Oncology, Beijing Cancer Hospital. Self-control comparative study on the antiemetic efficacy of aprepitant used or not in the chemotherapy was performed. At the same time, the maintenance of antiemetic effect of aprepitant was evaluated in multiple chemotherapy cycles. ResultsThe incidence of acute nausea and vomiting of granisetron and dexamethasone was 50.0%, while the incidence of delayed nausea and vomiting was 81.8%. The incidence of acute nausea and vomiting of aprepitant, granisetron and dexamethasone was 25.0%, while the incidence of delayed nausea and vomiting was 47.7%. The effective control rate of acute nausea and vomiting of aprepitant, granisetron and dexamethasone was 90.9%; while the effective control rate of delayed nausea and vomiting was 77.8%. The antiemetic effect of aprepitant was better in multiple chemotherapy cycles without significant difference. The main adverse reactions and their incidences caused by Aprepitant were anorexia, fatigue, constipation and diarrhea, respectively. These adverse reactions except for anorexia had significant differences before and after chemotherapy(P<0.05)through self-control comparative analysis. Conclusion Aprepitant can effectively reduce the incidence of acute and delayed nausea and vomiting caused by platinum-based chemotherapy and the adverse reactions were tolerable.

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